Literature DB >> 19961055

[C677T polymorphism of the methylentetrahydrofolate reductase gene as risk factor in women with recurrent abortion].

Alisandra Morales-Machín1, Lisbeth Borjas-Fajardo, José Miguel Quintero, William Zabala, Francisco Alvarez, Wilmer Delgado, María Luisa Hernández, Ernesto Solis-Añez, Yanira y Sánchez, Zoraida Butrón.   

Abstract

The pathogenesis of recurrent spontaneous abortion is multifactorial, presumably involving the interaction of several genetic and environmental factors. The methylenetetrahydrofolate reductase (MTHFR) gene C677T polymorphism has been implicated as risk factor for recurrent spontaneous abortion (RA). The main objective of this research was to investigate the association between the C677T polymorphism of the MTHFR gene as a genetic risk factor for idiopathic RA. Molecular analysis was performed in 80 DNA samples from 30 patients with RA and among 50 healthy control subjects. Using the Polymerase Chain Reaction (PCR), a 198 bp (bases pairs) fragment, was digested with the restriction enzyme Hinf1, which can recognize the C > T substitution responsible for the polymorphism. 677T MTHFR allele frequencies for group with RA and the control group were 35% and 33%, respectively and 677C MTHFR allele frequencies were 65% and 67%, respectively. There was no significant difference in allele frequency between these two groups. The data presented in this study fail to support the relationship between MTHFR C677T polymorphism and risk in women with RA.

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Year:  2009        PMID: 19961055

Source DB:  PubMed          Journal:  Invest Clin        ISSN: 0535-5133            Impact factor:   0.683


  2 in total

1.  Evidence of Paternal N5, N10 - Methylenetetrahydrofolate Reductase (MTHFR) C677T Gene Polymorphism in Couples with Recurrent Spontaneous Abortions (RSAs) in Kolar District- A South West of India.

Authors:  Shiny Vanilla; C D Dayanand; Pushpa F Kotur; Moideen A Kutty; Pradeep Kumar Vegi
Journal:  J Clin Diagn Res       Date:  2015-02-01

2.  Comparison of two preventive treatments for patients with recurrent miscarriages carrying a C677T methylenetetrahydrofolate reductase mutation: 5-year experience.

Authors:  Philippe Merviel; Rosalie Cabry; Emmanuelle Lourdel; Segolene Lanta; Carole Amant; Henri Copin; Moncef Benkhalifa
Journal:  J Int Med Res       Date:  2017-01-12       Impact factor: 1.671

  2 in total

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